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Comparison of opioid free and opioid based anaesthesia in patient undergoing thyroid surgery on post operative outcome

Comparison of opioid free and opioid based anaesthesia in patient undergoing thyroid surgery on post operative outcome: a prospective randomized study - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/064997
Enrollment
59
Registered
2024-04-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E079- Disorder of thyroid, unspecified

Interventions

Intervention1: Desaturation after extubation will be treated with oxygen supplementation of 5 to 10 L min via the nasal catheter: 48hrs Control Intervention1: patients will receive intravenous dexamet

Sponsors

Department of Anaesthesiology
Lead Sponsor
Operation Theater
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: All Patients of either sex aged 18- 60 years of ASA physical status I-II undergoing elective thyroid surgery under general anesthes giving written informed consent.

Exclusion criteria

Exclusion criteria: Huge Goiter causing tracheal compression or dyspnea Derranged thyroid function test Obstructive sleep apnea syndrome Epilepsy or seizures Pregnancy and breast feeding

Design outcomes

Primary

MeasureTime frame
The comparison of incidence of PONV (defined as experiencing any event of nausea, retching, or vomiting) during the first 48 hours postoperative among two groups.Timepoint: The comparison of incidence of PONV (defined as experiencing any event of nausea, retching, or vomiting) during the first 48 hours postoperative among two groups.

Secondary

MeasureTime frame
To compare the following among two groups- 1. Post operative pain assessed with VAS scores at rest and while coughing 2. Time and dose of total rescue analgesic required. 3. Sevearity of PONV using 4-point Likert scale. 4. Side effects among two groups Timepoint: 48hrs

Countries

India

Contacts

Public ContactDr Shefali Gautam

King Georges Medical University Lucknow

drshefaligautam@gmail.com9559468440

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026